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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2007-5-28
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pubmed:abstractText |
Autosomal dominant polycystic kidney disease (ADPKD) is a systemic disorder with a wide spectrum of renal involvement. Differences in the age at onset of end-stage renal disease (ESRD) are partially explained by the genetic heterogeneity of the disease but intrafamilial variability remains to be explained. Modifier genes may play a role in disease severity.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0931-0509
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1567-77
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17303584-Adult,
pubmed-meshheading:17303584-Disease Progression,
pubmed-meshheading:17303584-Female,
pubmed-meshheading:17303584-Humans,
pubmed-meshheading:17303584-Male,
pubmed-meshheading:17303584-Middle Aged,
pubmed-meshheading:17303584-Polycystic Kidney, Autosomal Dominant,
pubmed-meshheading:17303584-Polymorphism, Genetic,
pubmed-meshheading:17303584-Receptor, Bradykinin B1,
pubmed-meshheading:17303584-Receptor, Bradykinin B2,
pubmed-meshheading:17303584-Receptor, Epidermal Growth Factor,
pubmed-meshheading:17303584-Survival Analysis,
pubmed-meshheading:17303584-Transforming Growth Factor beta1
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pubmed:year |
2007
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pubmed:articleTitle |
Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1.
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pubmed:affiliation |
Hereditary Renal Diseases, Nephrology Department, Fundació Puigvert, Cartagena 340-350, 08025 Barcelona, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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